Custom-Made Zirconium Dioxide Implants for Craniofacial Bone Reconstruction

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Custom-Made Zirconium Dioxide Implants for Craniofacial Bone Reconstruction materials Article Custom-Made Zirconium Dioxide Implants for Craniofacial Bone Reconstruction Marcin Kozakiewicz 1,* , Tomasz Gmyrek 1 , Radosław Zajdel 2 and Bartłomiej Konieczny 3 1 Department of Maxillofacial Surgery, Medical University of Lodz, 113 Zeromskiego˙ Str, 90-549 Lodz, Poland; [email protected] 2 Department of Informatics and Statistics, Medical University in Lodz, Pl. Hallera 1, 90-647 Łód´z,Poland; [email protected] 3 University Laboratory of Materials Research, Medical University of Lodz, 251 Pomorska, 92-213 Lodz, Poland; [email protected] * Correspondence: [email protected]; Tel.: +48-42-639-3422 Abstract: Reconstruction of the facial skeleton is challenging for surgeons because of difficulties in proper shape restoration and maintenance of the proper long-term effect. ZrO2 implant application can be a solution with many advantages (e.g., osseointegration, stability, and radio-opaqueness) and lacks the disadvantages of other biomaterials (e.g., metalosis, radiotransparency, and no osseointe- gration) or autologous bone (e.g., morbidity, resorption, and low accuracy). We aimed to evaluate the possibility of using ZrO2 implants as a new application of this material for craniofacial bone defect reconstruction. First, osteoblast (skeleton-related cell) cytotoxicity and genotoxicity were determined in vitro by comparing ZrO2 implants and alumina particle air-abraded ZrO2 implants to the follow- ing: 1. a titanium alloy (standard material); 2. ultrahigh-molecular-weight polyethylene (a modern material used in orbital surgery); 3. a negative control (minimally cytotoxic or genotoxic agent action); 4. a positive control (maximally cytotoxic or genotoxic agent action). Next, 14 custom in vivo clinical ZrO2 implants were manufactured for post-traumatologic periorbital region reconstruction. The soft Citation: Kozakiewicz, M.; Gmyrek, tissue position improvement in photogrammetry was recorded, and clinical follow-up was conducted T.; Zajdel, R.; Konieczny, B. Custom-Made Zirconium Dioxide at least 6 years postoperatively. All the investigated materials revealed no cytotoxicity. Alumina Implants for Craniofacial Bone particle air-abraded ZrO2 implants showed genotoxicity compared to those without subjection to air Reconstruction. Materials 2021, 14, abrasion ZrO2, which were not genotoxic. The 6-month and 6- to 8-year clinical results were aesthetic 840. https://doi.org/10.3390/ma and stable. Skeleton reconstructions using osseointegrated, radio-opaque, personalized implants 14040840 comprising ZrO2 material are the next option for craniofacial surgery. Academic Editor: Matthias Kern Keywords: zirconium dioxide; custom implants; ultrahigh molecular weight polyethylene; titanium alloy; Received: 28 December 2020 craniofacial; maxillofacial surgery; cytotoxicity; genotoxicity; bone defect treatment Accepted: 7 February 2021 Published: 10 February 2021 Publisher’s Note: MDPI stays neutral 1. Introduction with regard to jurisdictional claims in The most common consequence (40%) of maxillofacial structure injuries is orbital re- published maps and institutional affil- iations. gion trauma [1]. If there is no complete reconstruction at the time of primary surgical repair, this may influence the outcomes. Facial skeleton fractures are often associated with the risk of functional disturbances (double vision and ptosis) as well as aesthetic disturbances (face asymmetry and enophthalmos) [1,2]. To date, no single ideal material is available to repair these post-traumatic defects and restore function. However, three options exist as ways to Copyright: © 2021 by the authors. shape the reconstructive material: 1. manually/arbitrarily; 2. individually on the model Licensee MDPI, Basel, Switzerland. but only for plastic materials possible; 3. design/manufacture of individual implants using This article is an open access article computer-assisted techniques—i.e., a final implant without model or manual shaping. distributed under the terms and conditions of the Creative Commons This third technique is the subject of this study. Attribution (CC BY) license (https:// Recently, custom-made implants have been prepared by computer-assisted design creativecommons.org/licenses/by/ (CAD) and manufacturing (CAM) for facial skeleton region reconstructions [3–7]. The goal 4.0/). of surgical reconstruction is to restore function and facial appearance. It is obtained by Materials 2021, 14, 840. https://doi.org/10.3390/ma14040840 https://www.mdpi.com/journal/materials Materials 2021, 14, 840 2 of 20 removing herniated tissues from the fracture gap, supporting the soft tissues and recon- structing the bone to prevent the return of the hernia. The most important issue in orbital reconstruction is obtaining the correct shape of the bone surface supporting the eye globe and skin, because an inaccurately corrected orbital volume causes unpleasant aesthetic consequences (enophthalmos). However, the type of material used, its properties, the cor- rectly designed shape of the implant, the appropriate surgical technique and the condition of the patient are all crucial for success. The material applied should be biocompatible and allow fixation to host bone by screws, wire, suture or adhesive. It should not potentiate the growth of microorganisms or promote resorption of the underlying bone or defor- mation of adjacent tissues. Furthermore, radiopaque materials should be used to allow radiographic evaluation [8]. Visibility in radiological examination allows confirmation of correct implantation. In the case of implant malposition detected in the intraoperative imaging scan, it allows for immediate correction of the position, avoiding a second surgery. The search continues for the ideal implant and reconstructive material, and particularly osseointegrated materials, such as titanium. Titanium is currently the standard material in craniofacial reconstructions; another material is zirconium dioxide. Zirconium dioxide (zirconia) is a ceramic material with physical properties that have long been appreciated in the space industry to cover shuttles and manufacture medical devices. In 1969, zirconium dioxide (ZrO2) material was first studied by orthopedics for hip head replacement [9]. Since 1985, ZrO2 has been applied to make the artificial head of the hip [10]. Its unusual break resistance (2000 N), compression resistance (2000 MPa) and biocompatibility have found their application in implantology to reconstruct missing teeth as well as hips, knees, shoulders and wrists [9]. Its mechanical properties are very similar to those of metals. MgO, CaO or Y2O3 interstitials are being added for greater molecular stability. The most studied combination is yttrium-stabilized zirconia, also known as tetrag- onal zirconia polycrystals. ZrO2 stabilized with Y2O3 has better mechanical properties than other combinations [9]. Despite a much more difficult process of sintering, this form of zirconia is considered for medical applications. Clinically, ZrO2 has several advantages over titanium. The inflammatory reaction to ZrO2 is much lower than that to other restorative materials, even titanium [10,11]. Evaluating soft tissues in contact with titanium and ZrO2 reveals a higher inflammatory reaction around titanium [12]. Additionally, in the case of titanium implanted during the treatment of trauma-related effects, changes in antioxidant defense and increased synthesis of the products of oxidative damage of proteins and lipids indicate the body’s adverse response to the introduction of titanium material [13]. Furthermore, the level of bacterial products measured using nitric oxide syntheses is higher on titanium than on zirconium dioxide [9]. The use of zirconium dioxide in craniofacial reconstruction has not been described in the literature thus far and appears very promising. The authors aimed to evaluate the cytotoxicity and genotoxicity of zirconium dioxide material as well as present a new application of that material for craniofacial bone defect reconstruction. 2. Materials and Methods In vitro-tested materials were formed in 2 mm-thick disks with diameters of 10 mm. Titanium alloy grade 23 powder (ISO 5832-3:1996 for selective laser melting) [14] was used in an SLM 250 machine (SLM Solutions GmbH, Lübeck, Germany). The thickness of the added layers in the implant was 30 µm (Z-axis move), and the construction speed was 25 cm3/h. Next, the disks were subjected to annealing at 700 ◦C for 1 h in an argon atmosphere, slowly cooled down in a furnace and subjected to the tempering process. Ten disks produced in this way created a comparison group as a standard material for craniomaxillofacial surgery. The next comparison group consisted of 10 disks milled from ultra-high-molecular- weight polyethylene (UHMW PE; [15–17]) in a computer numerical control (CNC) pro- cess [3] by Speed Hawk 650 (OPS-Ingersoll Funkenerosion GmbH, Burbach, Germany). Materials 2021, 14, 840 3 of 20 Zirconium dioxide disks were milled from prefabricated blocks (the substrate block Prettau Zyrconia of dimensions 125 mm × 70 mm × 20 mm was delivered by Zyrkonzahn Worldwide, Gais, Italy, https://www.zirkonzahn.com/ (accessed on 10 January 2021)). Twenty percent enlarged substrate disks were CAD designed, and CNCs were milled using a 5-axis milling machine [3] by Speed Hawk 650 (OPS-Ingersoll Funkenerosion GmbH, Bur- bach, Germany). Subsequently, sintering of substrate disks was performed at 1450–1500 ◦C according to the manufacture of zirconium dioxide substrate.
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